Job Title: Clinical System LeaderJob Description

The Clinical Systems Leader is responsible for implementing all related clinical systems actions used in the development of clinical trials within Early Clinical Development. The role requires collaboration with a cross-functional team of internal stakeholders and technology vendors to ensure the successful implementation and maintenance of technology solutions supporting clinical trials.

ResponsibilitiesImplement all related clinical systems such as Interactive Response Technologies (IxRS) and electronic Clinical Outcome Assessments (eCOA) actions for the ECD portfolio.Closely manage study-related timelines and associated activities.Lead the end-to-end specifications for the build of clinical systems for an assigned study or enterprise project, including requirements review, testing, deployment, maintenance, enhancement, and closeout.Provide technical oversight to ensure clinical systems solutions adhere to the study protocol, industry regulations, best practices, and company policies, procedures, and guidelines.Work independently with PET stakeholders and/or cross-functional project teams and collaboratively with the ECD IA team to share knowledge.Proactively identify and track study-level technical issues to resolution, ensuring prompt resolution of system issues, document issues and risks, and implement mitigation plans in partnership with the study team and technology vendor project manager.Communicate technical issues clearly, concisely, and professionally with internal and external stakeholders and departmental leadership.Essential SkillsBachelor's Degree in life science, computer science, engineering, information system, data science, or related discipline.2-5 years of experience in Clinical Operations or Clinical Systems Management.2-5 years of experience in IxRS/IRT and clinical-related systems.Successful track record in leading the implementation of clinical systems such as IxRS/IRT, ePRO, and eCOA.Working knowledge of Good Clinical Practices and FDA regulations governing clinical trial execution.Excellent written and verbal communication skills and strong project management skills.Additional Skills & QualificationsFamiliar with documentation in a regulated environment.Experience in Veeva is a plus.Work Environment

This role follows a hybrid working model with three days in the office and two remote days. Anchor days are Tuesday through Thursday.

Job Type & Location

This is a Contract position based out of South San Francisco, CA.

Pay and Benefits

The pay range for this position is $72.00 - $80.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in South San Francisco,CA.

Application Deadline

This position is anticipated to close on Feb 20, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.